NDC 60687-641 – Nebivolol

Nebivolol Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC60687-641

Product details

Brand name
Nebivolol
Generic name
Nebivolol
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203828
Marketed since
September 7, 2022
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Nebivolol →

Package NDC codes (1)

Package NDCDescriptionSince
60687-641-2130 BLISTER PACK in 1 CARTON (60687-641-21) / 1 TABLET in 1 BLISTER PACK (60687-641-11)Sep 7, 2022

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